Pentoxifylline

NDC 70954-668 · ANI Pharmaceuticals, Inc.

Generic namePentoxifylline

Dosage formTABLET, EXTENDED RELEASE

RouteORAL

Active ingredient(s)PENTOXIFYLLINE

Strength400 mg/1

Pharmacologic classBlood Viscosity Reducer [EPC], Hematologic Activity Alteration [PE]

Marketing categoryANDA

Packages

70954-668-10 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70954-668-10)

70954-668-20 — 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70954-668-20)

FDA lists these products with the same active ingredient.

0615-8511 — Pentoxifylline, 0904-5448 — PENTOXIFYLLINE, 16571-856 — Pentoxifylline, 60505-0033 — PENTOXIFYLLINE, 63629-2910 — PENTOXIFYLLINE, 71335-2586 — Pentoxifylline

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.